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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250818Generated: October 31, 2026

Ethylenediamine → HCID 18764906, compound

https://huagongshe.com/reaction/1250818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
Reactant2-PyridinecarboxaldehydeHCID 14273—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 18764906HCID 18764906—

Reaction Steps

This ligand was prepared according to a modified procedure described by Bernal et al in J. Chem. Soc., Dalton Trans, 22, 3667 (1995). First N,N′-bis(pyridin-2ylmethyl)-ethanediamine (bispicen) was synthesised by the following procedure. Ethylenediamine (26 ml, 0.38 mol) was dissolved in 200 ml dry methanol. To this mixture 74 ml (0.76 mol) pyridincarboxaldehyde was added. The mixture was refluxed for 2 h, after which the mixture was left to cool to RT and in small portions 40 g of NaBH4 was added. The mixture was subsequently stirred for 16 h at RT. The methanol was evaporated and 500 ml of water was added. The aqueous mixture was extracted with three portions of dichloromethane (100 ml) and the dichloromethane solution was dried over sodium sulphate, filtered off and the solvent was removed. The dark oil containing N,N′-bis(pyridin-2ylmethyl)-ethanediamine (73.7 g; 81%) was analysed by NMR and used without further purification. 1H-nmr (CDCl3): δ2.20 (br, NH); 2.78 (s, 4H); 3.85 (s, 4H); 7.00-7.40 (m, 4H); 7.58 (m, 2H); 8.45 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340661B1
Source datasetuspto-grants-2002_01
ORD IDord-c24ccac06e344cdb8d7cc7bb65f86f5c
Source noteuspto-grants-2002_01